(Q58417098)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15329069%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

title

Familial partial epilepsy with variable foci: clinical features and linkage to chromosome 22q12 (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15329069%20AND%20SRC:MED&resulttype=core&format=json

familial partial epilepsy

1 January 2020

main subject

1 reference

based on heuristic

inferred from title

epilepsy, familial focal, with variable foci

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15329069%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

Pilar Gómez-Garre

7

1 reference

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1 January 2020

Iscia Lopes-Cendes

11

1 reference

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1 January 2020

Robyn Wallace

15

1 reference

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1 January 2020

14

Ingrid E Scheffer

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15329069%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

5

Eva Andermann

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15329069%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

John Frederick Mulley

16

object named as

John C Mulley

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15329069%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

2

Jose M Serratosa

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15329069%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

17

Massimo Pandolfo

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15329069%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

13

Richard Desbiens

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15329069%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

author name string

Lan Xiong

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15329069%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

Frederick Andermann

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15329069%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

Francois Dubeau

12

1 reference

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1 January 2020

Hilary A Phillips

3

1 reference

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1 January 2020

Fernando Díaz-Otero

6

1 reference

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1 January 2020

Mercedes Martín

8

1 reference

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1 January 2020

Yolanda Fernández-Bullido

9

1 reference

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1 January 2020

publication date

1 September 2004

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15329069%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15329069%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

volume

45

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15329069%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

issue

9

1 reference

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1 January 2020

page(s)

1054-1060

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15329069%20AND%20SRC:MED&resulttype=core&format=json

Genetics of temporal lobe epilepsy

1 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.0013-9580.2004.30502.X

A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.0013-9580.2004.30502.X

The nicotinic receptor beta 2 subunit is mutant in nocturnal frontal lobe epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.0013-9580.2004.30502.X

Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.0013-9580.2004.30502.X

Mapping of a gene determining familial partial epilepsy with variable foci to chromosome 22q11-q12.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.0013-9580.2004.30502.X

Genetic linkage studies in familial frontal epilepsy: Exclusion of the human chromosome regions homologous to the El-1 mouse locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.0013-9580.2004.30502.X

Autosomal dominant nocturnal frontal-lobe epilepsy: genetic heterogeneity and evidence for a second locus at 15q24

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.0013-9580.2004.30502.X

The DNA sequence of human chromosome 22

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.0013-9580.2004.30502.X

10.1111/J.0013-9580.2004.30502.X

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15329069%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

1 reference